FDA.reportPublic FDA data

Borago Lavender cum Cupro

Manufacturer
Uriel Pharmacy, Inc.
Effective date
2021-10-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:30:17

Label at a glance#

ProductBorago Lavender cum Cupro
Active ingredientMELILOTUS INDICUS SEED, CUPRIC SULFATE, BORAGE, HORSE CHESTNUT
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Apply to skin as needed. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: 100gm contains: 20gm Aesculus (Horse chestnut seed) 1X, 20gm Borago (Borage) 1X, 13gm Melilotus (Yellow sweet clover) 1X, 40gm Cuprum sulfuricum (Copper sulfate) 2X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, Witch hazel extract, Magnesium aluminum silicate, Lavender oil, Silica gel, Sorbic acid, Tea tree oil, Xanthan gum, Grapefruit seed extract

OTC - PURPOSE SECTION

Uses: Temporarily relieves symptoms of varicose veins and leg cramps.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: FOR EXTERNAL USE ONLY.
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist,
or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. May leave a therapeutic white residue of silica.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Borago Lavender cum Cupro LotionBorago Lavender cum Cupro Lotion

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-214348951-2143-5

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
MELILOTUS INDICUS SEEDF22I9R6Q0XACTIB
LAVENDER OILZBP1YXW0H8IACT
TEA TREE OILVIF565UC2GIACT
CUPRIC SULFATELRX7AJ16DTACTIM
XANTHAN GUMTTV12P4NEEIACT
BORAGEPB618V0K2WACTIB
HAMAMELIS VIRGINIANA TOP WATERNT00Y05A2VIACT
WATER059QF0KO0RIACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
SORBIC ACIDX045WJ989BIACT
HORSE CHESTNUT3C18L6RJAZACTIB
CITRUS PARADISI SEED12F08874Y7IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2178571b-6824-f2d6-e063-6294a90ab639cf5b6661-8a2d-2084-e053-2a95a90a1c922024-09-06WarningsExact identifier
spl set id: cf5b6661-8a2d-2084-e053-2a95a90a1c92

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.